IL212845A - Assessing a subject's circulatory system - Google Patents

Assessing a subject's circulatory system

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Publication number
IL212845A
IL212845A IL212845A IL21284511A IL212845A IL 212845 A IL212845 A IL 212845A IL 212845 A IL212845 A IL 212845A IL 21284511 A IL21284511 A IL 21284511A IL 212845 A IL212845 A IL 212845A
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IL
Israel
Prior art keywords
sensor
subject
flexible substrate
signals
posture
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IL212845A
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Hebrew (he)
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IL212845A0 (en
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Dialog Devices Ltd
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Application filed by Dialog Devices Ltd filed Critical Dialog Devices Ltd
Publication of IL212845A0 publication Critical patent/IL212845A0/en
Publication of IL212845A publication Critical patent/IL212845A/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/0205Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/026Measuring blood flow
    • A61B5/0261Measuring blood flow using optical means, e.g. infrared light
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/026Measuring blood flow
    • A61B5/0295Measuring blood flow using plethysmography, i.e. measuring the variations in the volume of a body part as modified by the circulation of blood therethrough, e.g. impedance plethysmography
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/103Detecting, measuring or recording devices for testing the shape, pattern, colour, size or movement of the body or parts thereof, for diagnostic purposes
    • A61B5/11Measuring movement of the entire body or parts thereof, e.g. head or hand tremor, mobility of a limb
    • A61B5/1116Determining posture transitions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00Apparatus for radiation diagnosis, e.g. combined with radiation therapy equipment
    • A61B6/50Clinical applications
    • A61B6/504Clinical applications involving diagnosis of blood vessels, e.g. by angiography
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/06Measuring blood flow

Description

ASSESSING A SUBJECT'S CIRCULATORY SYSTEM Dialog Devices Limited C. 209467 TITLE Assessing a subject's circulatory system.
FIELD OF THE INVENTION Embodiments of the present invention relate to assessing a subject's circulatory system.
BACKGROUND TO THE INVENTION The response of a subject's circulation system to a subject's posture change may depend upon characteristics of the blood such as its viscosity, characteristics of the circulation system such as its resistance and how the autonomous nervous system responds to maintain homeostasis.
Blood perfusion at a periphery may, for example, be dependent upon one or a combination of the following factors:- 1. vascular disease such as for example Raynaud's disease 2. genetic problems such as for example scleroderma 3. an abnormal vasoconstriction or vaso-dilation response from the autonomous nervous system instigated by for example diabetic neuropathy or alcoholism 4. drug treatments such as for example Beta blockers . auto-immune diseases such as for example Lupus It will therefore be appreciated that there may be many reasons why a subject's circulatory system response to a postural change may be "abnormal". Different pathologies may have the same or different effects on circulation.
It would be desirable to provide an interim clinical indicator that characterizes a response of the circulation system to a series of postural changes and provides a clinician with information which in combination with other information and the clinician's skill and knowledge may be used to assess whether or not pathology may be present. The medical practitioner can then, using his own medical knowledge, conduct independent investigations before identifying any pathology.
BRIEF DESCRIPTION OF VARIOUS EMBODIMENTS OF THE INVENTION According to various, but not necessarily all, embodiments of the invention there are provided methods, systems, apparatuses and computer programs as claimed as the appended claims.
According to various, but not necessarily all, embodiments of the invention there is provided a system and method for assessing a subject's circulatory system using optical sensors and multiple postural changes.
This provides the advantage of low cost, rapid pain free assessment of subject physiology by assessment of disturbances to the circulatory system.
It should therefore be appreciated that the present invention does not diagnose a disease but provides an interim clinical indicator which is of a type that is not dissimilar to body temperature, blood pressure, heart rate etc.
BRIEF DESCRIPTION OF THE DRAWINGS For a better understanding of various examples of embodiments of the present invention reference will now be made by way of example only to the accompanying drawings in which: Fig 1 schematically illustrates a system comprising: optical sensors and an apparatus; Fig 2 illustrates the apparatus in more detail; Fig 3 schematically illustrates an artificial neural network for producing a metric; Figs 4A and 4B illustrate different implementations of a flexible substrate for sensors; Figs 5A, 5B and 5C schematically illustrate safety features for flexible substrates.
DETAILED DESCRIPTION OF VARIOUS EMBODIMENTS OF THE INVENTION Functional tests are used to provoke changes in the circulatory system of a subject. Functional test involves placing the subject into different postures and recording data at those postures. The exact number, type, order, frequency of postures used in a particular functional test protocol is predetermined and depends upon the subject's physiology and pathology under investigation.
A kinematic protocoi (or test) is a sequence of three or more different postures. The sequence is typically carried out in a single continuous session. The sequence may be carried out as an uninterrupted sequence that does not have significant hiatus between postural changes.
The different postures adopted during a kinematic protocol may for example include at least three of: a reference posture, none, one or more 'local' (or 'limb') postures, none, one or more 'orthostatic' (or 'torso') postures, and none, one or more 'systemic' (or 'whole body') postures.
In a 'local' (or 'limb') posture, a limb has been moved through a gravitational field relative to a stationary body torso.
In a Orthostatic' (or 'torso') posture, the body torso has been moved through a gravitational field relative to a stationary limb or limbs (e.g. legs).
In a 'systemic' {or 'whole body') posture, the whole body has been moved within a gravitational field but without relative movement between the body torso and limbs. This may be achieved by inclining a stationary subject.
The at least three different postures result in at least two different postural changes. The postural changes are changes of the whole or parts of the body relative to a gravitational field. The different postural changes therefore result in different 'impulses' to the subject's circulatory system.
It may be desirable to have a first type of impulse such as a 'local' (or 'limb') impulse by changing to a 'local' (or 'limb') posture or an 'orthostatic' (or 'torso') impulse by changing to an 'orthostatic' (or 'torso') posture or a 'systemic' (or 'whole body') impulse by changing to a 'systemic' (or 'whole body') position. It may be desirable to also have a different second type of impulse. Therefore if the first type of impulse was 'local' (or 'limb') the second type of impulse may be 'orthostatic' (or 'torso') or 'systemic' (or 'whole body') but not 'local' (or 'limb').
The following kinematic protocol can be used to assess a local response of a capillary bed i.e. vaso-dilation and vaso-contraction. A local postural change is followed by a systemic postural change.
First the local postural change is performed. An initial reference posture in which a subject is supine and an arm is level with the heart may be followed by a local posture in which the subject is supine and the arm is vertically displaced below the heart.
Then a systemic postural change is performed. An initial reference posture in which a subject is supine and an arm is level with the heart may be followed by a systemic posture in which the angle of incline of the body is changed without independent movement of the arm relative to the torso so that the head is vertically displaced below the heart.
A sensor may be located on an index finger of the arm. This sensor may be an optical transmission sensor which is sensitive to the arterial blood volume.
A sensor may be located on the forearm or the back of the hand. This sensor may be an optical reflection sensor which is sensitive to skin venous blood volume changes. The skin reflection sensor also permits normalizing of the digit transmission sensor caused by venous blood volume changes.
The outputs from the sensors have characteristics that produce different patterns as the kinematic protocol is performed. The patterns for a normal circulatory response share a common distinctive pattern. This distinctive pattern may be determined theoretically or empirically and then used to pattern match the outputs from the sensors for a subject during the same kinematic test. A metric may be output that indicates whether or the degree of pattern matching. A pattern match indicates a normal circulatory response for the given kinematic test. A pattern mismatch indicates an abnormal circulatory response that merits further investigation.
The following kinematic protocol can be used to assess arterial blood supply to the brain. An orthostatic (or body) postural change is followed by a systemic postural change.
First the orthostatic (or body) postural change is performed. The subject is initially in a supine reference position to record a baseline. The subject sits up or is sat up to an orthostatic (or body) posture, which would cause blood flow to the brain to initially reduce due to orthostatic pressure changes.
Then the systemic postural change is performed., The subject is returned to the supine reference position to record a baseline. The subject in the supine position is tilted so that the angle of incline of the body is changed so that the head is vertically displaced below the heart.
A sensor may be located on the subject's forehead. This sensor may be an optical reflection sensor which is sensitive to localized venous blood volume caused by pooling.
A sensor may be located across the nose. This sensor may be an optical transmission sensor which is sensitive to the arterial blood volume which is dependent upon the interior carotid artery via the ophthalmic and ethmoidal arteries.
A sensor may be located on an ear lobe. This sensor may be an optical transmission sensor which is sensitive to the arterial blood volume which is dependent on the external carotid artery via the temporal artery.
The sensors are preferably at approximately the same height to avoid orthostatic compensation.
The outputs from the sensors have characteristics that produce different patterns as the kinematic test is performed. The patterns for a normal circulatory response share a common distinctive pattern. This distinctive pattern may be determined theoretically or empirically and then used to pattern match the outputs from the sensors for a subject during the same kinematic test. A metric may be output that indicates whether or the degree of pattern matching. A pattern match indicates a normal circulatory response. A pattern mismatch indicates an abnormal circulatory response that merits further investigation such as a Magnetic Resonance Imaging (MRI) Scan if compromised blood supply to the brain is a possibility.
Fig 1 schematically illustrates a system 10 comprising: optical sensors 2A, 2B, 2C and an apparatus 20.
The sensors 2A, 2B and 2C are positioned at respective locations 4A, 4B, 4C of a subject's body. In the example illustrated, the sensors 2A and 2B are attached to a substrate 6 and the substrate 6 is attached to the subject's body 8.
The sensors are non-invasive sensors typically photo sensors such as optical transmission sensors and/or optical reflection sensors. The sensors are for sensing physiological attributes such as, for example, changes in the volume of the body (plethysmography). An optical sensor comprises a light emitter and photo-detector. In a transmission sensor, in use, the photo-detector is positioned to receive light from the light emitter that has passed through the subject's body 8. In a reflection sensor, in use, the photo-detector is positioned to receive light from the light emitter that has been reflected by the subject's body 8.
It should be appreciated that the sensors 2A, 2B provide inputs to the apparatus 20 throughout the kinematic protocol i.e., for each posture of the subject.
Although only a single sensor is illustrated at each location, it should be appreciated that multiple sensors may be implemented at each location. For example, combinations of reflectance and transmission sensors may be provided in the same iocation. Also sensors that operate at different wavelengths of light may also be positioned at the same location. A sensor operating in near infrared of around 850nm would be weakly affected by absorption in tissue but strongly affected by absorption by blood and could for example be used to monitor the reaction of a capillary bed during a kinematic test. Whereas a sensor operating around 650nm would be strongly affected by absorption in tissue and could for example be used to monitor the reaction of skin tone during a kinematic test. The signal from the 850nm sensor would have a much larger arterial component than the 650nm sensor as it would penetrate deeper into tissue.
The sensors communicate with the apparatus 20 either using wireless methods (ZigBee, Bluetooth, UHF radio etc) or cables.
The apparatus 20 comprises an input interface 22 that pre-processes signals received from the sensors 2A, 2C and provides signal 23 to processing circuitry 24. The processing circuitry 23 is configured to determine and output a metric 25 by combining, according to pre-defined calibration data 28 the provided signals 23.
In the example illustrated, the provided signals 23 dependent upon blood presence at a first, second and third locations 4A, 4B, 4C when a subject is in the different postures of the kinematic protocol.
The interface 22 may also perform some signal processing before providing the signals 23 to the processing circuitry 24.
For example, the interface may separate an intensity signal from a sensor into two distinct signals having different frequency components. For example, it may produce an 'ac signal' that relates to the time varying intensity recorded at a sensor and a 'dc signal' that measures the quasi-static intensity recorded at the senor.
As another example, the interface 22 may apply a non-linear function such as a logarithmic function to the signals 23 before they are provided to the processing circuitry 24.
The processing circuitry 24 may be implemented in any suitable manner. It may, for example, be a programmable computer or dedicated hardware. The interface 22 may be implemented in any suitable manner. It may, for example, comprise a programmable computer or dedicated hardware.
It should be appreciated that the interface 22 and processing circuitry may not be discrete physical components but may be functional modules implemented by common circuitry such as a processor executing different software modules.
The calibration data 2B is used to assess divergence of the provided signals 23 from an expected pattern of signals that characterize an expected response of a normalized circulation system to the kinematic protocol. The expected response may be an average of a statistical model of expected signals produced for example using machine learning.
The calibration data defines a non-linear combination of the signals. There will typically be different non-linear combinations of the signals 23 required for different kinematic tests as any pattern to be matched will vary with the location and type of sensors used and with the kinematic test performed. There will therefore be different calibration data 28 for each kinematic test.
Referring to Fig 2, the interface 22 comprises interface components 22A etc for one of the sensors 2A, however only the interface component 22A for the sensor 2A is illustrated. It should be appreciated that there will be an equivalent interface component.
The interface component 22A comprises analogue front end signal processing circuitry 32 for processing the intensity signal received from the sensor 2A and at least one Analogue to Digital converter 34.
There may be multiple front ends intended for simultaneous continuous monitoring of multiple sensors, or a single front end with an appropriate multiplexor switch. The front end circuitry may provide for constant control of the current provided to the sensors, trans-impedance amplification of the received signals 30, compensation for ambient light interference. This may be achieved using time division multiplexing (TDM), in which the periods where a light source is not illuminated, allows monitoring of ambient light interference. This may alternatively be achieved using frequency division implemented by employing a modulated light source and a frequency locking or demodulation system.
The front end circuitry 32 may initialize the sensors by configuring itself for a mid-scale value of the semi-static signal component by varying the LED intensity so the resultant signal would be mid way between a desired range, again for example unity. Any signal increases or decreases would be accommodated within the signal ranges, reducing the likelihood of signal saturation or diminishment.
In the example illustrated, the interface component 22A separates the received signal 30, after pre-processing, into two distinct signals 35, 36 having different frequency components.
It may produce an ac signal 36 by passing the received signal 32 through a high pass filter 38. The ac signal 36 relates to the time varying intensity recorded at a sensor. It may also produce a dc signal 35 by passing the received signal 32 through a low pass filter 42 that integrates, typically with a time constant of several seconds. The dc signal 35 relates to a quasi-static intensity recorded at the sensor. Filtering could be performed either in hardware using conventional linear time invariant filters or after digitization within a microprocessor using digital filters such as Finite impulse response designs. Digital filtering has the advantage of being able to change the filter parameters via software update if required.
The signal or signals (if high and low pass filtering has occurred) would then be fed to an analogue to digital converter (ADC) 35 before being provided to the processing circuitry 24. The ADC may be a discrete item or may be contained in a microprocessor.
A logarithmic function may be applied to signals before they are processed by the processing circuitry 24 to produce the metric 25. This logarithmic function may be applied in the analogue or digital domain. If applied in the digital domain, it may be applied by the interface 22 or the processing circuitry 24.
Optical absorption spectroscopy can be modeled using the Lambert-Beer Law, in which received optical intensity is proportional to an exponential function that has as its argument the product of a one dimensional optical path length and an absorption coefficient. Taking the natural logarithm of the received intensity produces a result that is linear in the optical path length. The optical path length may be assumed to vary depending on tissue blood volume, which is affected by posture and arterial dilation responses.
The processing circuitry in the illustrated example comprises a processor 40, a memory 42, a display 44 and a network interface 46. The processor 40 is configured to read from and write to the memory 42, to provide output commands to the display 44 and to communicate using the network interface 46.
The processor 40 would typically execute a program 48 from a memory 42 to calculate a metric 25 and then display the metric 25 on display 44.
The computer program may arrive at the apparatus via any suitable delivery mechanism. The delivery mechanism may be, for example, a computer-readable storage medium, a computer program product, a memory device, a record medium such as a CD-ROM or DVD, an article of manufacture that tangibly embodies the computer program. The delivery mechanism may be a signal configured to reliably transfer the computer program.
The exact form of the algorithm for a multi sensor, multi posture kinematic test is typically a summation of non-linear weighted input signals S 23. Some statistical manipulation may occur on the signals 23 before input to the algorithm. For example the median of a dc signal 35 may be calculated whereas a root mean squared value may be calculated for the ac signal 36.
The algorithm weights may be set using a-priori knowledge, or training using a teaching pattern and altering the weights according to the error.
If there are multiple postures i, multiple sensor sites j and multiple sensor wavelengths k at each sensor site, then the metric y could be defined as: y =∑∑∑c≠]°ss≠ where gn is the input signal 23 for posture /, at site j for wavelength k.
Calculation of the weights c is possible using regression analysis. A multi posture kinematic test would be performed on a range of subjects who would also undergo independent clinical assessment. Then a least squares regression analysis of the recorded inputs against an idealized metric permits the algorithm weights to be defined.
Alternatively the metric could be defined as an arbitrary weighted summation of nonlinear functions of the input signals ^ using an artificial neural network 50 such as, for example, schematically illustrated in Fig 3.
Artificial Neural Networks (ANN) are a class of non-linear weighting algorithms. The feed forward representation as illustrated in Fig 3 consists of a directed acyclic graph of interconnected nodes 52 arranged in layers 54A, 54B, 54C.
The feed forward network 50 illustrated in Fig 3 with three layers of neurons. Each input signal 23A, 23B, 23C, 23D is sent to every neuron 52 in an input layer 54A. Each neuron 52 in the input layer 54A forms its own weighted sum of its inputs 23A-D and provides the sum as an output. Each neuron 52 in the input layer 54A has its output connected to every neuron 52 in a hidden layer 54B. Each neuron 52 in the hidden layer 54B forms its own weighted sum of its inputs and provides the sum as an output. Each neuron 52 in the hidden layer 54B has its output connected to every neuron 52 in an output layer 54C. Each neuron 52 in the output layer 54C forms its own weighted sum of its inputs and multiplies the weighted sum by an activation function to produce the metric 25.
The metric 25 may be constrained to be a continuous value between 0 and 1 using a sigmoid function as the activation function, or between -1 and 1 using a hyperbolic tangent (Tanh) function as the activation function. If the metric is to be discrete, then a signum or step function could be used as the activation function.
In some implementations two layers 54 of neurons 52 may suffice.
The various weights applied in the weighted summations may be determined using supervised learning and back propagation. Alternatively optimum weights may be found using a genetic algorithm. The weights are comprised in the calibration data 28.
If there are / input nodes, j hidden nodes and only a single output node, the metric may be defined as Wherein /iv are > Note that x, represents a vector of statistic for the corresponding Sensor {SL.m) pulsatile component (AC) and quasi-static (DC) signal components for the different wavelengths ( j..„) for each posture (Ρ,..?).
The weights are defined using a training algorithm. Training, like in the simple algorithm above, requires known training data to be fed to the ANN, and the weights are modified using an error function or learning rule.
The network 50 would be trained by providing it with the input signal values for the postures obtained from a kinematic test and then matching using back propagation would be used to reduce an error between the output metric and an expected metric.
The steps for back propagation of ANN supervised learning may include: - 1. Present known training inputs to the ANN. 2. For each output neuron in the output layer, compare the ANN output metric to the expected metric for that known training sample and calculate the local error. 3. For each output neuron adjust the weights to lower the local error. 4. Assign different contributions for the local error to the neurons in the hidden layer, giving greater responsibility to neurons connected by stronger weights.
. Repeat the steps 3 and 4 for the neurons in the hidden layer using each one's responsibility as its error.
It will be appreciated from the above that the metric is sensitive to the location of a sensor and the order and nature of the postures in a kinematic test.
To enable the correct order and nature of the postures to be performed for a kinematic test corresponding to the current calibration data 28, the apparatus 20 may give instructions either via a display 44 or by synthesizing a voice. The instructions would indicate when and how a posture of a subject should be changed.
There will be different sets of calibration data for different kinematic tests. A menu may be provided to select a particular test. The correct calibration data 28 would then be loaded for use by the apparatus 20 along with the instructions telling the operative how to perform the kinematic test.
It is also important that the sensors are located accurately and applied to a subject in a manner that does not arbitrarily interfere with the signals 23.
Figs 4A and 4B illustrate two different examples of apparatus 60 having flexible substrates 62 that are suitable for applying sensors to a subject 8.
The apparatus 60 illustrated comprises an economically shaped flexible substrate 62.
At one end 64 of the flexible substrate 62 are located light emitter(s) and photo-detectors) in an adjacent configuration in order to act as a reflection sensor 66.
An adhesive collar 68 that surrounds and closely circumscribes the reflectance sensor 66 is used to attach the end 64 of the flexible substrate 62 to the subject. The collar 68 is preferably substantially opaque at the wavelengths at which the photo-detector operates so that it acts to isolate the photo-detector from ambient light. The adhesive collar may be shaped like an annulus. The adhesive collar 68 may be formed from hydrogel.
A second portion 70 of the flexible substrate 62 is folded to act as a transmission sensor 72- a light emitter(s) 72A is applied to one side of a protuberance and a photo-detector(s) 72B is applied on the other side of the protuberance.
An adhesive collar 68 that surrounds and closely circumscribes the light emitter 72A and an adhesive collar 68 that surrounds and closely circumscribes the photo-detector 72B are used to attach the end 70 of the flexible substrate 62 to the subject. The adhesive collar circumscribes in the sense that it surrounds but it does not necessarily touch. The collars 68 are preferably substantially opaque at the wavelengths at which the photo-detector operates so that it acts to isolate the photo-detector from ambient light. The adhesive collar may be shaped like an annulus. The adhesive collar 68 may be formed from hydrogel.
The adhesive collars 68 adhere sensors in the correct strategic place and they avoid the use of a mechanical clip system, which would compress the arteries and veins in the bridge of the nose. This is especially important for reflectance sensors as they are sensitive to a vasodilatory response that would be masked by mechanical compression.
Conductive interconnects feed from an edge connector 74 (where the embedded contacts are exposed from within the flexible substrate and are inserted into a spring leaf type metal contact, one for each connector) to the ends 64, 70 of the flexible substrate 62, communicating with the light sources and photo-detectors.
Referring to Fig 4A the flexible substrate 62 has a Ύ or T shape. The end 62 is located at the forehead of the subject. The end 70 is folded over the bridge of the nose to act as a transmission sensor.
The distance between the bridge of the nose and the reflection sensor on the head may be adjusted using a buckle (not shown), typically located between the eye brows which is only possible using a flexible substrate that will conform around the buckle. Alternatively the flexible substrate may be allowed to arch in order to accommodate excess length, as the hydrogel annulus adhesive should firmly affix the active components of the non-invasive optical sensors against the skin. The flexible substrate would typically be disposed of after use on a single subject to maintain hygiene and avoid subject cross contamination.
Referring to Fig 4B the flexible substrate 62 has a Ύ or T shape. The end 62 is located over the extensor digitorum brevis muscle, located over the region of the third cuneiform, cuboid and metatarsal bones of the foot. The end 70 of the substrate 62 would wrap over the end of the locating toe (typically second toe). The transmission light emitter 72A is applied to the nail matrix and the transmission photo-sensor 72B is applied to the pad of the second toe, diametrically opposite the emitter 72A.
During application of the sensor to the subject, the flexible substrate is designed to conform to the subject's foot, naturally following the contours of the foot in order to locate over the second toe. The flexible substrate is shaped to follow the curvature of the foot, approximating a T shape which is easily achieved by stamping and laminating in conductive elements.
The advantages of the adhesive fixation method are that hydrogel adhesion locates the sensors in the correct strategic places on the foot rather than using mechanical clip systems or loops around the diameter of the toe. The arteries feeding the pulp of the toe pass alongside the side of the toe; therefore any method of securing the toe sensor which employs fastenings around the toe could compress the arteries and veins, spoiling the effects of the postural test. This is especially important if a vasodilatory response is to be observed as these mechanical effects would mask the homeostasis response.
In addition, adhesive pads may be located at strategic points along the flexible substrate to stabilize the substrate and reduce sensor movement and resultant motion artifact.
The flexible substrate 62 illustrated in Fig 5B can with minor modification be made suitable for use with a hand. The reflectance sensor is located on the back of the hand and the transmission sensor is located on the index finger.
An alternative embodiment of this flexible substrate sensor would employ sensor elements on both sides of the substrate, permitting the substrate to be utilized on either foot.
Handedness detection A connecting cable connects with the edge conductor 74. The connecting cable has a series of contacts which are connected (perhaps semi-permanently) through the cable to particular parts of the front end circuitry 32. Consequently, the arrangement of the contacts at the interface of the connecting cable has, at least initially, a specific, predefined dedicated order. Thus a dedicated contact is always used to energize a first sensor and a dedicated contact is always used to receive.
Thus for example the following simplified table may illustrate a first correspondence between the contacts of the cable and those of the edge connector.
Table 1 The following simplified table may illustrate a second correspondence between the contacts of the cable and those of the edge connector.
Table 2 It is possible for the front end circuitry 32 to determine which of these configurations is used by applying an output LED control signal on only cable contact 1. If an input is received at the front end circuitry 32 on connector contact 2 then the first configuration is in use whereas if an input is received at the front end circuitry 32 on connector contact 4 then the second configuration is in use.
The different configurations may be used to identify different substrates 62.
Alternatively, the same substrate may be reversible with the first configuration used on one side and the second configuration used on the other side. This would enable the front end circuitry to determine the handedness of the substrate i.e. whether it is applied to a left or right foot. The front-end circuitry may then for example change how it provides signals to the substrate and how it interprets signals from the substrate.
It would also be possible to add redundant and/or degenerate contacts to create different configurations.
It is therefore possible to have a collection of flexible substrates where each substrate is economically configured to be applied to a different body part of a subject. Each substrate may comprise the same {or different) sensors and will have a set of interconnects supported by the flexible substrate that connect to the sensors. Each substrate will also have an interface comprising a common fixed physical configuration of interface connectors (connector contacts) for connecting the interconnects to remote processing circuitry via the cable. An ordering of the interconnects with respect to the common fixed physical configuration of interface connectors is dependent upon the body part to which a flexible substrate is to be applied. The ordering of the interconnects with respect to the common fixed physical configuration of interface connectors is uniquely indicative, when the flexible substrate is in use, to the processing circuitry of the body part to which the flexible substrate is attached.
Safety Control Referring to Figs 5A, 5B and 5C, the flexible substrate 62 may have a score or partial cut 90 (kiss-cut) through close to the designated edge connector 74. The width of the score may be across the whole of a tab supporting the edge connector 74 or more typically across 90% the width, leaving some of the substrate un-scored. The scoring produces a localized structural weakness controlled by the depth of the score, the cross section of the substrate and the tensile strength of the substrate material.
The interconnects 80 connecting the edge connector 74 to sensors may be formed from conductive ink, the thickness of the ink is tightly controlled, so the cross sectional area is less in the width of the score, but still sufficient to carry the appropriate current.
The design of the connecting cable's distal end female edge connector 94 includes a spring loaded retainer 92 which engages with a notch 83 on the side of the substrate male edge connector 74, or alternatively the cable edge connector includes a spring loaded detent pin which engages with a hole in the substrate close to the exposed edges of the connector tab. These features are designed into an edge connector shroud and are inaccessible by the user. The preferred method would use a small section of Printed Circuit Board (PCB) as a chassis, with the edge connector mounted and soldered to the PCB with through hole pins, where a piece of spring steel formed to act as the retaining lever is also soldered to the PCB. The cable shroud then serves to protect and form a substantial, rigid enclosure which can accept the force of the retainer and force of the operator.
When the kinematic test is complete, the operator removes the substrate 62 from the subject in the conventional way. The sensor is removed from the subject as normal, but for the substrate 62 to be removed from the cable edge connector, the substrate must be firmly grasped and pulled in order to overcome the spring loaded retainer 92 located in the edger connector shroud. At this moment the substrate section with the score will break, fracturing the interconnects 80. The score 90 runs transversely across some or all of the interconnects 80.
As the substrate is only partially scored, a section of the substrate will still remain intact, holding the tab to the remaining substrate. This prevents the substrate from breaking into two and the edge connector tab from getting stuck in the female edge connector.
To further facilitate this, the substrate is formed as a laminate of two layers 81 A and 81 B that are folded about join 83 and adhered together (Fig 5A). Less or no adhesive glue is applied between the layers where the layer 81 A has a score 90. In this embodiment, the score is made only in the laminate layer 81 A supporting the interconnects. The portion of this laminate layer 81 A demarcated by the score breaks away and may detach (Fig 5C). The retainer is however now no longer in effect, and the retained portion may be easily removed from the female edge connector.
The other laminated layer 81 B underlying the detachable portion 87 of the laminate layer 81 A may be colored 89 e.g. red. When the portion 87 of the laminate layer 81 A detaches severing the interconnects 90, the underlying colored layer 89 is exposed. This would indicate to the user that the substrate 62 has been used and should be disposed.
This method of fracturing the conductive ink conductors is far superior to the accidental, possibly intermittent, fractured conductor produced by material fatigue reuse, since the proposed method for producing the fractured electrical conductor is defined and reliable. Attempting to reuse a substrate with fractured conductors would be detected by the front end circuitry 32 when it performs the standard self tests when initializing for a kinematic test. For example, detecting insufficient power being consumed by the LEDs indicates fracture in the LED conductor lines.
For additional security, a programmable component such as a fusible fink may also be incorporated as part of the conductive ink inside the sensor, which permits a sensor to be marked as 'used' by the system after the test. The fusible link can be effected by carefully controlling the screen printing process to deliver a conductive ink section with a known cross sectional area for a given maximum power dissipation. A short electrical pulse substantially exceeding this maximum power dissipation would controllably disrupt the fusible link, leaving it open circuit. The fusible link would be brought out to an additional edge connector conductor, or would be part of the existing tracking inside the sensor.
The blocks illustrated in the Figs may represent steps in a method and/or sections of code in the computer program. The illustration of a particular order to the blocks does not necessarily imply that there is a required or preferred order for the blocks and the order and arrangement of the block may be varied. Furthermore, it may be possible for some steps to be omitted.
Although embodiments of the present invention have been described in the preceding paragraphs with reference to various examples, it should be appreciated that modifications to the examples given can be made without departing from the scope of the invention as claimed.
Features described in the preceding description may be used in combinations other than the combinations explicitly described.
Although functions have been described with reference to certain features, those functions may be performable by other features whether described or not.
Although features have been described with reference to certain embodiments, those features may also be present in other embodiments whether described or not.
Whilst endeavoring in the foregoing specification to draw attention to those features of the invention believed to be of particular importance it should be understood that the Applicant claims protection in respect of any patentable feature or combination of features hereinbefore referred to and/or shown in the drawings whether or not particular emphasis has been placed thereon. l/we claim :

Claims (42)

1. An apparatus comprising: an input interface configured to provide signals from at least two sensors for at least two postures including: signals, dependent upon blood presence, from a first sensor when a subject is in a first posture; signals, dependent upon blood presence, from the first sensor when the subject is in a second posture; signals, dependent upon blood presence, from a second sensor when the subject is in the first posture; and signals, dependent upon blood presence, from the second sensor when the subject is in the second posture; and processing circuitry configured to determine and output a metric by combining, according to pre-defined calibration data the provided signals.
2. An apparatus as claimed in claim 1 , wherein the signals, for each combination of sensor and posture, comprises at least one logarithm of detected light intensity.
3. An apparatus as claimed in claim 1 or 2, wherein the signals, for each combination of sensor and posture, include separately a time varying component of detected light intensity and a quasi static component of detected light intensity.
4. An apparatus as claimed in any preceding claim, wherein the signals, for each combination of sensor and posture, include separately a logarithm of a time varying component of detected light intensity and a logarithm of a quasi static component of the detected light intensity.
5. An apparatus as claimed in any preceding claim, wherein the signals, for each combination of sensor and posture, include a signal based upon a light intensity signal detected at an optical reflectance sensor and a signal based upon a light intensity signal detected at an optical transmission sensor.
6. An apparatus as claimed in any preceding claim, wherein the signals, for each combination of sensor and posture, include a signal based upon a light intensity signal detected at a first wavelength but not at a second wavelength and a signal based upon a light intensity signal detected at at least the second wavelength but not the first wavelength.
7. An apparatus as claimed in any preceding claim, wherein the calibration data is used to assess divergence of the provided signals from an expected average of a statistical model of expected signals to produce the metric,
8. An apparatus as claimed in any preceding claim, wherein the calibration data defines a non-linear combination of the signals.
9. An apparatus as claimed in any preceding claim, wherein the calibration data is predetermined using machine learning.
10. An apparatus as claimed in any preceding claim, configured to emulate an artificial neural network comprising a plurality of nodes each of which has associated weights for inputs to the node, wherein the calibration data provides said weights.
11. An apparatus as claimed in any preceding claim, further comprising a memory storing multiple sets of calibration data comprising a set of calibration data for each of a plurality of predetermined standard sequences of different body postures.
12. An apparatus as claimed in any preceding claim, wherein at least one of the sensors provide signals from optical reflection detectors
3. An apparatus as claimed in any preceding claim, wherein a change from the first posture to the second posture is expected to cause a local, as opposed to systemic, circulatory reaction
14. An apparatus as claimed in any preceding claim, wherein a change from the first posture to the second posture causes, for the subject, a relative vertical displacement with respect to the subject's heart of a subject's peripheral limb of without relative vertical displacement with respect to the subject's heart of the subject's head.
15. An apparatus as claimed in claim 14, wherein at least the first sensor is on the limb.
16. An apparatus as claimed in any one of claims 1 to 15, wherein a change from the first posture to the second posture is expected to cause a systemic circulatory reaction.
17. An apparatus as claimed in any one of claims 1 to 11 or 16, wherein a change from the first posture to the second posture causes, for the subject, a relative vertical displacement with respect to the subject's heart of the subject's head.
18. An apparatus as claimed in claim 17, wherein at least the first sensor is on the subject's head.
19. An apparatus as claimed in claim 18, wherein the first sensor provides signals from an optical transmission sensor.
20. An apparatus as claimed in any preceding claim, wherein the metric records a divergence of the signals from an expected pattern of signals that characterize an expected response of a normalized circulation system to the predetermined sequence of first and second postures.
21. A system comprising: an apparatus as claimed in any preceding claim; and at least a first sensor and a second sensor.
22. A system as claimed in claim 21 , wherein the first sensor is at a first location and the second sensor is at a second, different, location.
23. A system as claimed in claim 21 or 22, wherein the first sensor detects light at a first wavelength but not at a second wavelength and the second sensor detects light at the second wavelength but not at the first wavelength.
24. A system as claimed in claim 21 , 22 or 23 wherein the first sensor is a reflectance sensor and is attached without clamping using an opaque adhesive collar that closely circumscribes the reflectance sensor.
25. A system as claimed in any one of claims 21 to 24, wherein the first sensor and second sensor are attached to a flexible substrate comprising interconnects that are connectable to the apparatus via an interface, wherein a portion of the flexible substrate, underlying one or more of the interconnects, has a manufactured structural weakness and wherein, in use, the portion of the flexible substrate having the structural weakness connects with the interface which retains the substrate against removal such that on attempted removal of the flexible substrate from the interface the manufactured structural weakness breaks the one or more interconnects.
26. A system as claimed in claim 25, wherein the interface additionally detaches a portion of the flexible substrate to reveal an indicator.
27. A system as claimed in any one of claims 21 to 26, wherein the first sensor and second sensor are attached to a flexible substrate for application to a subject and are connectable to the processing circuitry via a first set of interconnects embedded in the flexible substrate, wherein an ordering of the interconnects embedded in the substrate is dependent upon whether the flexible substrate is for use on a right limb or a left limb and wherein the ordering of the interconnects embedded in the substrate, in use, is indicative to the processing circuitry of whether the flexible substrate is applied to a right limb of the subject or a left limb of the subject.
28. A system as claimed in any one of claims 21 to 27, wherein the first sensor and second sensor are attached to a first side of a flexible reversible substrate and are connectable to the processing circuitry via a first set of interconnects on the first side of the flexible substrate and wherein a third sensor and a fourth sensor are attached to a second side of the flexible substrate and are connectable to the processing circuitry via a second set of interconnects on the second side of the flexible substrate, wherein an ordering of the first set of interconnects across the first side of the flexible interconnect, when the first side of the flexible substrate is upwards facing, is different to an ordering of the second set of interconnects across the first side of the flexible substrate when the second side of the flexible substrate is upwards facing thereby enabling the processing circuitry to determine which side of the reversible flexible substrate is operational.
29. A system as claimed in any one of claims 21 to 28, wherein first signals detected by the first sensor are processed to produce parallel signals that have different frequency components before combination at the processing circuitry and wherein second signals detected by the second sensor are processed to produce parallel signals that have different frequency components before combination by the processing circuitry.
30. A system for assessing a subject's blood circulation a first detector configured to detect signals dependent upon blood presence when the subject is in a first posture and when the subject is in a second posture; at least one other detector configured to detect signals dependent upon blood presence when the subject is in the first posture and when the subject is in the second posture; and processing circuitry configured to determine a metric by combining the detected signals from the first and second detectors for the first and second postures according to calibration data.
31. A method comprising: attaching optical sensors to a subject; connecting the optical sensors to an apparatus as claimed in any one of claim 1 to 20; moving the subject through a predetermined ordered sequence of different postures including the first and second postures.
32. A method as claimed in claim 31 , wherein the optical sensors are attached by attaching a disposable flexible substrate to the subject.
33. A method as claimed in claim 32, wherein the disposable flexible substrate is attached to a limb and comprises at least one optical reflectance sensor.
34. A method as claimed in claim 33, wherein the flexible substrate is attached using adhesive only and without the use of a clamping force.
35. A method as claimed in claim 32, wherein the disposable flexible substrate is attached to a subject's head and comprises at least one optical transmission sensor.
36. A method comprising: processing light intensity signals received from optical sensors positioned on a subject when the subject is moved through a predetermined sequence of at least three different postures according to a kinematic protocol to provide input signals; combining the input signals to produce and output a metric that quantitatively defines a response of the subject's circulatory system to the predetermined sequence of at least three different postures of the kinematic protocol.
37. An apparatus comprising: a flexible substrate; a first optical sensor at a first location on the flexible substrate arranged in a reflectance configuration and a first adhesive collar closely circumscribing the first optical sensor, a second optical sensor at a second location on the flexible substrate; and a second adhesive collar closely circumscribing the second optical sensor, wherein the first adhesive collar is configured to position the first sensor adjacent a subject's body for physiological sensing and wherein the second adhesive collar is configured to position the second sensor adjacent the subject's body for physiological sensing.
38. An apparatus comprising: a flexible substrate comprising a manufactured structural weakness; at least a first sensor and a second sensor attached to the flexible substrate ; interconnects connected to the first and second sensors; and an interface for connecting the interconnects to a cable, wherein the manufactured structural weakness underlies one or more of the interconnects adjacent the interface.
39. An apparatus comprising: a reversible flexible substrate having a first side and an opposing second side; a first sensor and a second sensor attached to the first side of the reversible flexible substrate ; a first set of interconnects, on the first side of the reversible flexible substrate, connected to the first and second sensors in a first order; a third sensor and a fourth sensor attached to the first side of the reversible flexible substrate ; a second set of interconnects, on the second side of the reversible flexible substrate, connected to the third and fourth sensors in a second order; wherein the first order of the first set of interconnects across the first side of the flexible interconnect, when the first side of the flexible substrate is upwards facing, is different to the second order of the second set of interconnects across the second side of the flexible substrate when the second side of the flexible substrate is upwards facing.
40. An apparatus comprising: a flexible substrate for application to a subject, the flexible substrate comprising at least a first sensor and a second sensor; a set of interconnects supported by the flexible substrate and connected to the sensors; an interface for connecting the interconnects to remote processing circuitry; wherein an ordering of the interconnects is dependent upon whether the flexible substrate is for use on a right limb or a left limb and wherein the ordering of the interconnects is indicative, when the apparatus is in use, to the processing circuitry of whether the flexible substrate is applied to a right limb of the subject or a left limb of the subject.
41. A collection of flexible substrates wherein each flexible substrate is economically configured to be applied to a different body part of a subject, and comprises: at least a first sensor and a second sensor; a set of interconnects supported by the flexible substrate and connected to the sensors; an interface comprising a common fixed physical configuration of interface connectors for connecting the interconnects to remote processing circuitry; wherein an ordering of the interconnects with respect to the common fixed physical configuration of interface connectors is dependent upon the body part to which a flexible substrate is to be applied and wherein the ordering of the interconnects with respect to the common fixed physical configuration of interface connectors is uniquely indicative, when the flexible substrate is in use, to the processing circuitry of the body part to which the flexible substrate is attached.
42. An apparatus comprising: an input interface configured to provide signals dependent upon blood presence at at least two locations for at least two postures including signals dependent upon blood presence at a first location when a subject is in a first posture, signals dependent upon blood presence at the first location when the subject is in a second posture, signals dependent upon blood presence at a second location when the subject is in the first posture, and signals dependent upon blood presence at the second location when the subject is in the second posture; processing circuitry configured to determine and output a metric by combining, according to pre-defined calibration data the provided signals. por the App!loante KINHOLD COHN AMD PARTNERS By I
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